光谱式染色体自动核型分析简介
被引量:1
A review of SKY( Spectral Karyotyping)
摘要
光谱染色体自动核型分析(SKY -SpectralKaryotying)是近年来在国际上迅速发展的一项技术。自问世以来 ,即以其检测灵敏度高 ,操作简单等优势得到了广泛应用 ,在我国部分医院也已经开始应用该项技术。本文从SKY技术的原理、发展前景、优越性以及与同类技术的性能比较等方面对该技术进行了介绍。
出处
《医疗设备信息》
2002年第5期45-46,共2页
Information of Medical Equipment
参考文献8
-
1[1]Abdel- Rahman WM, Katsura K, Rens W, Gorman PA, Sheer D, Bicknell D, Bodmer WF, Arends MJ, Wyllie AH, and Edwards PA. Spectral karyotyping suggests additional subsets of colorectal cancers characterized by pattern of chromosome rearrangement. Proc Natl Acad Sci U S A, 2001, 98(5): 2538- 2543.
-
2[2]Aben KK, Macville MV, Smeets DF, Schoenberg MP, Witjes JA and Kiemeney LA. Absence of karyotype abnormalities in patients with familial urothelial cell carcinoma. Urology, 2001, 57(2): 266- 269.
-
3[3]Adeyinka A, Kytola S, Mertens F, Pandis N and Larsson C. Spectral Karyotyping and chromosome banding studies of primary breast carcinomas and their lymph node metastases. Int. J Mol Med. March, 2000, 5 (3): 235- 240.
-
4[4]Allen RJ, Smith SD, Moldwin RL, Lu MM, Giordano L, Vignon C, Suto Y, Harden A, Tomek R, Veldman T, Ried T, Larson RA, Le Beau MM, Rowley JD and Zeleznik- Le N. Establishment and characterization of a megakaryoblast cell line with amplification of MLL. Leukemia, 1998, 12: 1119- 1127.
-
5[5]Ariyama Y, Fukuda Y, Okuno Y, Seto M, Date K, Abe T, Nakamura Y and Inazawa J. Amplification on double- minute chromosomes and partial- tandem duplication of the MLL gene in leukemic cells of a patient with acute myelogenous leukemia. Genes Chromosomes Cancer, 1998, 23: 267- 72.
-
6[6]Ariyama Y, Sakabe T, Shinomiya T, Mori T, Fukuda Y and Inazawa J. Identification of amplified DNA sequences on double minute chromosomes in a leukemic cell line KY821 by means of spectral karyotyping and comparative genomic hybridization. J. Hum. Genet, 1998, 43: 187- 190.
-
7[7]Bamard M, Bayani J, Grant R, Teshima I, Thorner P and Squire J. Use of multicolor spectral karyotyping in genetic analysis of pleuropulmonary blastoma. Pediatr Dev Pathol, 2000, 3: 479- 486.
-
8[8]Bayani J and Squire JA. Advances in the detection of chromosomal aberrations using spectral karyotyping. Clin Genet, 2001, 59(2): 65- 73.
同被引文献11
-
1Rauman JG, Wiegant J, Wiegant P, et al. A new method for fluorescence microscopical localization of specific DNA sequences by in situ hybridization of fluorochrome - labelled RNA[ J ]. Exp Cell Res, 1980, 128:485~490.
-
2Hook EB. The impact of aneuploidy up on public health: Motiality and mobidity associated with human chromosome abnormality[M] .New York: Plenum Press, 1985.7 ~ 33.
-
3Xu J, Fong CT, Cedrone E, et al. Prenatal indentification of de novo maker chromosomes using micro - FISH approach [ J ]. Clic Genet,1998,53(6) :490 ~ 496.
-
4Rajgopal A, Carr IM. Detection by fluorescence in situ hybridization of microdeletions at 1p36 in lymphomas, unidentified on cytogenetic analysis[J]. Cancer Genetics & Cytogenetics,2003,142(1):46 ~ 50.
-
5Marinescu RC, Grad YD, Chen XN, et al. FISH analysis of terminal deletions in patients diagnosed with cri-du-chat syndrome[J]. Clin Genet,1999,56(4) :282 ~ 288.
-
6Ruault M, Brun ME, Ventura M, et al. MLL3, a new human member of the TRX/MLL gene family, maps to 7q36,a chromosome region frrequently deleted in myeloid leukaemia[J]. Gene,2002,284(1):73~ 81.
-
7Shan ZH,Zabel B,Trautmann U,et al. FISH mapping of the sex-reversal region on human chromosome 9p in two XY females and in primates[C].Euro J Hum Genet,2000.167~ 173.
-
8Bryce LA,Morrison N.Mapping of the gene for the human telomerase reverse transcriptase, hTERT,to chromosome 5p15.33 by fluorescence in situ hybridization[C]. Neoplsaia,2000.198 ~ 202.
-
9Trask BJ, Massa H, Kennrick S, et al. Mapping of human chromosome Xq28 by two-colour fluorescence in situ hybridization of DNA sequences to interphase cell nuclei[J] .Am J Hum Genet, 1991,48:1 ~ 15.
-
10谭跃球,李秀蓉,李麓芸,卢光琇.一个涉及1号和7号染色体插入易位家系的鉴定[J].中华医学遗传学杂志,2001,18(3):183-186. 被引量:5
-
1陈晓宁.在基因组的“深海”中钓鱼(FISHing)[J].生命的化学,1999,19(1):6-8.
-
2汪亚平,刘焕章.鲂成体组织及胚胎发育过程中同工酶表达的研究[J].Zoological Research,1994,15(S1):107-118. 被引量:2
-
3薛渊博,宋鑫.肿瘤染色体畸变分析方法新进展[J].遗传,2008,30(12):1529-1535. 被引量:1
-
4李劲松,汤富酬,徐国良.哺乳动物受精卵中雌雄原核DNA去甲堪化机制的研究[J].科学新闻,2015,0(1):50-50.
-
5徐路生.光谱核型分析技术及其应用[J].国外医学(遗传学分册),1999,22(4):207-214. 被引量:2
-
6周桂娜,陈宝安.M-FISH技术在复杂核型异常的急性白血病患者的诊断、预后分析中的应用[J].中国实验血液学杂志,2010,18(1):246-249. 被引量:2
-
7张入元,张慧娟.一类非线性差分方程存在正解的充分条件[J].经济数学,2000,17(2):72-76.
-
8常顺,李池陶,石连玉.不同品系镜鲤鱼种的生长性能比较[J].饲料博览(技术版),2008(12):28-30. 被引量:1
-
9张子平,王艺磊.中国对虾两个种群的F_1的LDH和MDH同功酶初步分析[J].热带海洋,1994,13(1):87-90. 被引量:10
-
10吴慧利,唐义,白廷柱,蒋玉蓉,蒋静.紫外薄膜光学常数的多层模型椭偏测量[J].光电工程,2015,42(9):89-94. 被引量:2